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Pulmonary Arterial Hypertension: Pathophysiology and Treatment

Pulmonary arterial hypertension (PAH), the first category of pulmonary hypertension, is a chronic and progressive disorder characterised by angioproliferative vasculopathy in the pulmonary arterioles, leading to endothelial and smooth muscle proliferation and dysfunction, inflammation and thrombosis...

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Detalhes bibliográficos
Publicado no:Diseases
Main Authors: Lan, Norris S. H., Massam, Benjamin D., Kulkarni, Sandeep S., Lang, Chim C.
Formato: Artigo
Idioma:Inglês
Publicado em: MDPI 2018
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6023499/
https://ncbi.nlm.nih.gov/pubmed/29772649
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/diseases6020038
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